Cited by 104Bipolar Disorder and TreatmentCircadian rhythm and melatoninSleep and related disorders

Sleep- and circadian rhythm–associated pathways as therapeutic targets in bipolar disorder

Open access
Bellivier, Frank, Geoffroy, Pierre-Alexis, Etain, Bruno, Scott, Jan·2015·Expert Opinion on Therapeutic Targets

Abstract

INTRODUCTION: Disruptions in sleep and circadian rhythms are observed in individuals with bipolar disorders (BD), both during acute mood episodes and remission. Such abnormalities may relate to dysfunction of the molecular circadian clock and could offer a target for new drugs. AREAS COVERED: This review focuses on clinical, actigraphic, biochemical and genetic biomarkers of BDs, as well as animal and cellular models, and highlights that sleep and circadian rhythm disturbances are closely linked to the susceptibility to BDs and vulnerability to mood relapses. As lithium is likely to act as a synchronizer and stabilizer of circadian rhythms, we will review pharmacogenetic studies testing circadian gene polymorphisms and prophylactic response to lithium. Interventions such as sleep deprivation, light therapy and psychological therapies may also target sleep and circadian disruptions in BDs efficiently for treatment and prevention of bipolar depression. EXPERT OPINION: We suggest that future research should clarify the associations between sleep and circadian rhythm disturbances and alterations of the molecular clock in order to identify critical targets within the circadian pathway. The investigation of such targets using human cellular models or animal models combined with 'omics' approaches are crucial steps for new drug development.

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Crossref · 10.1517/14728222.2015.1018822

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  • Genetic linkage studies have been equivocal, yet modest associations have been reported between bipolar disorder and multiple genes of the molecular circadian clock.

    “Genetic linkage studies have been equivocal115, yet modest associations have been reported between BD and multiple genes of the molecular circadian clock116,117.”

    From Circadian rhythm disruption and mental health (2020) · cites this paper as [117]

  • Dysregulation of, or certain polymorphisms in, associated genes involved in the circadian molecular clock may increase susceptibility to develop bipolar disorder and also influence circadian phenotypes which could lead to relapse into episodes.

    “Dysregulation of, or certain polymorphisms in, the afore associated genes involved in the circadian molecular clock may increase susceptibility to develop BD and also influence circadian phenotypes which could lead to relapse into episodes117.”

    From Circadian rhythm disruption and mental health (2020) · cites this paper as [117]

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References 200 · Cited by 104

Authors
Bellivier, F., Geoffroy, P.-A., Etain, B., & Scott, J.
Affiliations
  • Inserm (FR)
  • Newcastle University (GB)
Venue
Expert Opinion on Therapeutic Targets
Published
2015-03-02
Volume
19
Issue
6
Pages
747-763
ISSN
  • 1472-8222 (ISSN-L)
  • 1744-7631
OpenAlex
W2322240666
Cited by
104
References
200
Citations by year
2026: 5 · 2025: 7 · 2024: 6 · 2023: 12 · 2022: 13 · 2021: 8 · 2020: 13 · 2019: 7 · 2018: 9 · 2017: 10 · 2016: 12 · 2015: 2
FWCI
1.48
Type
journal article
Language
en
Open access
Locations
  • Expert Opinion on Therapeutic Targets (publishedVersion)
  • PubMed (publishedVersion)
  • Newcastle University ePrints (Newcastle Univesity)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
Keywords
bipolar disorder, sleep disorders, circadian rhythm disruption, circadian clock, lithium, pharmacogenetics, sleep deprivation, phototherapy, bipolar depression, biomarkers, therapeutic target
MeSH terms
Animals, Bipolar Disorder, Circadian Rhythm, Humans, Pharmacogenetics, Polymorphism, Genetic, Sleep Wake Disorders, Drug Design, Lithium Compounds, Chronobiology Disorders, Molecular Targeted Therapy

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